Archives: Conditions A-Z

Autoimmune hepatitis

Chronic immune-mediated liver inflammation responsive to immunosuppression.

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Bartter syndrome

Salt-wasting tubulopathy of the thick ascending limb with hypokalemic metabolic alkalosis.

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Alport syndrome

Type IV collagen disorder with progressive nephritis, hearing loss and ocular changes.

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Autosomal dominant polycystic kidney disease

Commonest inherited kidney disease with progressive cyst growth and renal failure.

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Alpha-1 antitrypsin deficiency

An underdiagnosed genetic cause of lung and liver disease; augmentation therapy is available for selected patients.

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Brugada syndrome

Inherited arrhythmia syndrome with characteristic ECG and risk of sudden death.

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Arrhythmogenic right ventricular cardiomyopathy

Fibrofatty replacement of myocardium causing ventricular arrhythmias and sudden death, especially in athletes.

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Castleman disease

Lymphoproliferative disorder ranging from unicentric to multicentric inflammatory disease.

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